Cowden Syndrome with Cortical Malformation and Epilepsy

J Gordon Millichap

doi:10.15844/pedneurbriefs-27-1-10

Cowden Syndrome with Cortical Malformation and Epilepsy

Pediatric Neurology Briefs

Volume 27 (2013): Issue 1

By: J Gordon Millichap

Open Access

|Jan 2013

Abstract

Investigators at the Institute for Research on Mental Retardation and Brain Aging, Troina, and University of Naples, Italy report a case of Cowden syndrome presenting with unilateral perisylvian dysplasia and with drug resistant focal seizures.

References

Elia M Amato C Bottitta M Grillo L Calabrese G Esposito M An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy Brain Dev 2012 Nov 34 10 873 6 10.1016/j.braindev.2012.03.005 22469695
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Lloyd KM 2nd Dennis M Cowden's disease. A possible new symptom complex with multiple system involvement Ann Intern Med 1963 Jan 58 136 42 13931122
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-27-1-10 | Journal eISSN: 2166-6482

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Language: English

Page range: 7 - 7

Published on: Jan 1, 2013

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Cowden Syndrome,

Hamartomatous,

Lhermitte-Duclos Disease

© 2013 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 27 (2013): Issue 1